510(k) K990863 ยท KNT Tubes, Gastrointestinal (And Accessories)
MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE
| Applicant | Ross Product Div. Abbott Laboratories, Columbus OH, US |
| Decision | Substantially Equivalent, Apr 6, 1999 |
| Received | Mar 16, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990863
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.